| GENE NAME | MYH11 |
| CHROMOSOME | 16 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000133392 |
| UNIPROT ACCESSION NUMBER | P35749 |
| GO MOLECULAR FUNCTION | ['calmodulin binding', 'structural constituent of muscle', 'protein binding', 'cytoskeletal motor activity', 'actin filament binding', 'ATP binding'] |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa04270; hsa04530; hsa04810; hsa05130; hsa04270; hsa04530; hsa04810; hsa05130; R-HSA-1266738; R-HSA-162582; R-HSA-194315; R-HSA-195258; R-HSA-2682334; R-HSA-373755; R-HSA-3928663; R-HSA-397014; R-HSA-400685; R-HSA-416572; R-HSA-422475; R-HSA-445355; R-HSA-5625740; R-HSA-5625900; R-HSA-5627117; R-HSA-5627123; R-HSA-9675108 |
| 2 combinations linked to MYH11 | OLI330; OLI1802 |
| 2 variants linked to MYH11 | MYH11:c.5890G>C, p.Glu1964Gln; MYH11:c.5772G>C, p.Met1924Ile |
| 2 diseases linked to MYH11 | Hypoplastic left heart syndrome; Amyotrophic lateral sclerosis |